4.7 Article

Excellent performance of cobalt-impregnated activated carbon in peroxymonosulfate activation for acid orange 7 oxidation

Journal

ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 24, Issue 10, Pages 9651-9661

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11356-017-8648-7

Keywords

Peroxymonosulfate; Orange acid 7; Activated carbon; Cobalt; Chloride

Funding

  1. National Natural Science Foundation of China [51478283, 51509175]
  2. Brook Byers Institute for Sustainable Systems (BBISS)
  3. Hightower Chair
  4. Georgia Research Alliance at Georgia Institute of Technology

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Cobalt-impregnated activated carbon (GAC/Co) was used to produce sulfate radical (SO4 (center dot-)) from peroxymonosulfate (PMS) in aqueous solution (hereafter called PMS activation). We evaluated its effectiveness by examining the degradation of orange acid 7 (AO7). GAC/Co exhibited high activity to activate PMS to degrade AO7. The degradation efficiency of AO7 increased with increasing dosage of GAC/Co or PMS and elevated temperatures. pH 8 was most favorable for the degradation of AO7 by GAC/Co-activated PMS. The radical quenching experiments indicated that the reactions most likely took place both in the bulk solution and on the surface of GAC/Co. We found that SO4 (center dot-) played a dominant role in AO7 degradation. Sodium chloride (NaCl) which presents in most dye wastewater had a significant impact on AO7 degradation. Low dosages (< 0.4 M) of NaCl showed a slight inhibitory effect, whereas high dosages (0.8 M) increased the reaction rate. HOCl was confirmed as the main contributor for accelerating AO7 degradation with high concentration of NaCl. In a continuous-flow reaction with an empty-bed contact time of 1.35 min, AO7 was not detected in the effluent for 0 to 18.72 L of treated influent volume (156 h) and 85% removal efficiency was still observed after 40.32 L of treated volume (336 h). Finally, the azo bond and the naphthalene structure in AO7 were destroyed and the degradation pathway was proposed.

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